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Moderna

Develops mRNA-based medicines for health

Co-op

Business OperationsConfirmed live in the last 24 hours
Internship · Winter 2027Norwood, MA, USA

About the Job

Requirements

  • Currently enrolled in a Bachelor’s or Master’s degree program in Life Sciences, Business, Engineering, Quality, Healthcare Administration, or a related field.
  • Proficiency with Microsoft Office applications, particularly Word, Excel, and PowerPoint, and an interest in learning digital collaboration and workflow tools.
  • Applicants must already hold U.S. work authorization and be able to maintain that status without future sponsorship.
  • Applicants must qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) to access export-controlled information.

Responsibilities

  • Support innovation and digital enablement efforts by gathering user needs, documenting current-state workflows, testing proposed solutions, and preparing user guidance or training materials under team supervision.
  • Collaborate with cross-functional partners to explore practical uses of automation, dashboards, and approved AI-enabled tools for document management, knowledge sharing, and process efficiency, and summarize findings and recommendations.
  • Gain exposure to approved Generative AI tools and help evaluate how they may support more efficient information access, knowledge sharing, documentation, and digital ways of working within applicable company frameworks.
  • Contribute to process mapping, workflow documentation, and continuous improvement projects, including identifying opportunities to simplify manual steps and enable more efficient digital processes.
  • Support the drafting, formatting, and revision of standard operating procedures, work instructions, and related controlled documents using established templates and guidance.
  • Assist with quality control reviews of controlled documents for clarity, consistency, formatting, cross-references, and alignment with applicable document standards.
  • Help maintain and enhance document trackers, action logs, dashboards, and project status reports to support controlled document development, digital visibility, and implementation.
  • Assist with document lifecycle, training, and digital workflow activities in systems such as Veeva Quality, Smartsheet, and Microsoft 365 tools, according to assigned access and training.
  • Support the organization and analysis of process documentation, training matrices, and related records to identify gaps and opportunities for improvement.
  • Work with process, training, and cross-functional partners to support consistent execution and adoption of new or improved processes and digital tools across Development.
  • Contribute to projects that improve how teams access information, manage documentation, and execute work in a regulated, quality-focused clinical development environment.

Desired Qualifications

  • A GPA of 3.5 on a 4.0 scale or equivalent academic achievement.
  • Clear written and verbal communication skills, including an interest in technical writing and document editing.
  • High attention to detail, with an interest in process quality, consistency, and continuous improvement.
  • Curiosity about digital tools, workflow automation, data visualization, or responsible use of AI to improve business processes; prior experience is a plus but not required.
  • Interest in clinical development operations, regulated processes, quality systems, training, process improvement, innovation, or digital transformation.

About the Company

Moderna

Develops mRNA-based medicines for health

Moderna develops medicines built on messenger RNA (mRNA). Its products use mRNA delivered into cells to instruct them to produce specific proteins that can prevent or treat disease, with vaccines being a primary example. In practice, a dose delivers engineered mRNA into the body, cells translate it into a target protein, and the immune system responds or the protein modulates biology to combat disease. Moderna differentiates itself through its focus on building a whole mRNA medicines platform and in-house capabilities for designing, manufacturing, and scaling mRNA therapies, including rapid development and large-scale production. Its goal is to create a new category of medicines based on mRNA that can improve how diseases are discovered, developed, and treated, ultimately improving patient outcomes.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2010

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